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抗狂犬病单克隆抗体鸡尾酒疗法SYN023在暴露后预防动物模型中的体内疗效

In Vivo Efficacy of SYN023, an Anti-Rabies Monoclonal Antibody Cocktail, in Post-Exposure Prophylaxis Animal Models.

作者信息

Chao Tzu-Yuan, Zhang Shou-Feng, Chen Li, Tsao Eric, Rupprecht Charles E

机构信息

Synermore Biologics Co., Ltd., 6F-6, No. 5, Aly. 22, Ln. 513, Ruiguang Rd., Neihu Dist., Taipei 11492, Taiwan.

Laboratory of Epidemiology and Key Laboratory of Jilin Provincial Zoonosis Control and Prevention, Military Veterinary Research Institute, Academy of Military Medical Sciences, 666 Liuying West Road, Jingyue Economic Development Zone, Changchun, Jilin 130122, China.

出版信息

Trop Med Infect Dis. 2020 Feb 21;5(1):31. doi: 10.3390/tropicalmed5010031.

DOI:10.3390/tropicalmed5010031
PMID:32098049
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7157742/
Abstract

Rabies immune globulin (RIG) is an indispensable component of rabies post-exposure prophylaxis (PEP) because it provides passive immunity to prevent this otherwise inescapably fatal disease in Category III exposed patients. Even with decades of development, RIG products are still criticized for their high cost, lot-to-lot variation, and potential safety issues. They remain largely unattainable in most developing regions of the world, where demand is highest. In recent years, monoclonal antibodies (MAbs) have become widely accepted as safer and more cost-effective alternatives to RIG products. As an example, SYN023 is a 1:1 cocktail of two humanized anti-rabies MAbs previously shown to display extensive neutralizing capabilities. Here, we further assessed the efficacy of SYN023 in animal models of rabies, and found that SYN023 afforded protection equal to a standard dose of human RIG (HRIG) at 0.03 mg/kg in Syrian hamsters and 0.1 mg/kg in beagles. Potential interference with vaccine-induced immunity was analyzed for the MAbs at these concentrations. While individual MAbs did not interfere with vaccine response, SYN023 at dosages of 0.1 mg/kg and above resulted in reduced neutralizing antibody titers similar to HRIG. Thus, the in vivo characterization of SYN023 supports its utility in human rabies PEP as an efficacious alternative to RIG products.

摘要

狂犬病免疫球蛋白(RIG)是狂犬病暴露后预防(PEP)中不可或缺的组成部分,因为它能提供被动免疫,以预防III级暴露患者感染这种否则将不可避免导致死亡的疾病。即使经过数十年的发展,RIG产品仍因成本高、批次间差异大以及潜在的安全问题而受到批评。在世界上大多数需求最高的发展中地区,它们仍然基本上无法获得。近年来,单克隆抗体(MAb)已被广泛接受为比RIG产品更安全、更具成本效益的替代品。例如,SYN023是两种人源化抗狂犬病单克隆抗体的1:1混合物,此前已显示具有广泛的中和能力。在此,我们进一步评估了SYN023在狂犬病动物模型中的疗效,发现在叙利亚仓鼠中,0.03mg/kg剂量的SYN023和在比格犬中0.1mg/kg剂量的SYN023提供的保护等同于标准剂量的人狂犬病免疫球蛋白(HRIG)。分析了这些浓度下单克隆抗体对疫苗诱导免疫的潜在干扰。虽然单个单克隆抗体不干扰疫苗反应,但0.1mg/kg及以上剂量的SYN023会导致中和抗体滴度降低,类似于HRIG。因此,SYN023的体内特性支持其作为RIG产品的有效替代品在人类狂犬病PEP中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bf/7157742/a817a1084f75/tropicalmed-05-00031-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bf/7157742/7523c3dfb3f7/tropicalmed-05-00031-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bf/7157742/7cf9e2dfe667/tropicalmed-05-00031-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bf/7157742/a817a1084f75/tropicalmed-05-00031-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bf/7157742/7523c3dfb3f7/tropicalmed-05-00031-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bf/7157742/7cf9e2dfe667/tropicalmed-05-00031-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bf/7157742/a817a1084f75/tropicalmed-05-00031-g003.jpg

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